QA Validation Engineer

Job Opportunity: QA Validation Engineer
Location: Swindon
Contract Type: Temporary (Inside IR35)
Duration: 3 to 6 months (with potential for extension)
Working Pattern: Full Time, 40 hours per week, 8:30am - 5:00pm (30-minute unpaid lunch break)
Hourly Rate: £26.44 - £31.23 per hour (equivalent to £55,000 - £65,000 per annum)
Start Date: ASAP

Are you ready to take your career to the next level in the dynamic world of pharmaceuticals? Our client is urgently seeking a QA Validation Engineer with a passion for ensuring top-notch quality in sterile pharmaceutical manufacturing! Join a vibrant team in Swindon and make a significant impact on a high-profile project.

What You'll Do:
As a QA Validation Engineer, you will be at the forefront of quality assurance within a sterile manufacturing environment. Your responsibilities will include:

• Reviewing and Assessing: Evaluate CQV documentation for equipment used in sterile manufacturing.
• Compliance Checks: Ensure all documentation meets cGMP, FDA, and other relevant regulatory standards.
• Identifying Issues: Spot gaps, discrepancies, and non-conformities in validation documents.
• Recommending Solutions: Propose corrective actions and quality enhancements.
• Collaborating: Work closely with Engineering, QA, and Operations teams to resolve documentation challenges.
• Maintaining Records: Keep accurate, timely records of document reviews.
• Staying Updated: Keep abreast of evolving regulatory and industry best practises related to sterile manufacturing.

What You Bring:
To thrive in this role, you'll need:

• Proven experience in CQV within sterile pharmaceutical manufacturing.
• Strong understanding of FDA, EMA, and cGMP guidelines.
• Exceptional attention to detail along with strong analytical and problem-solving skills.
• Effective communication abilities, both written and verbal.
• Capability to work independently while managing multiple priorities.
• Experience with document management and quality systems.
• Familiarity with risk-based validation approaches.

Why Join Us?

• Immediate Impact: Your expertise is needed now!
• Dynamic Environment: Work in a fast-paced, regulated atmosphere where your contributions matter.
• Professional Growth: Potential for contract extension based on your performance and project needs.
• Competitive Compensation: Enjoy a competitive hourly rate and the opportunity for future engagements.

If you're ready to make a difference and bring your strong sterile pharmaceutical manufacturing CQV experience to a vibrant team, we want to hear from you!

Apply today for immediate consideration! Your next exciting career opportunity awaits!

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